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Jhih-Rong Lin

Showing results (21-30 of 31) with videos related to

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Nature Metabolism|July 29, 2020
Genetics of extreme human longevity to guide drug discovery for healthy ageingZhengdong D Zhang, Sofiya Milman, Jhih-Rong Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Polygenic prediction of human longevity on the supposition of pervasive pleiotropyM Reza Jabalameli, Jhih-Rong Lin, Quanwei Zhang, et al.
Scientific Reports|August 28, 2024
Polygenic prediction of human longevity on the supposition of pervasive pleiotropyM Reza Jabalameli, Jhih-Rong Lin, Quanwei Zhang, et al.
Cell Reports|November 10, 2021
Genomic expansion of Aldh1a1 protects beavers against high metabolic aldehydes from lipid oxidationQuanwei Zhang, Gregory Tombline, Julia Ablaeva, et al.
Developmental Neuroscience|October 13, 2024
Ultrarare Variants in DNA Damage Repair Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome or Acute Behavioral Regression in Neurodevelopmental DisordersJanet L Cunningham, Jennifer Frankovich, Robert A Dubin, et al.
Molecular Psychiatry|March 3, 2023
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophreniaJhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, et al.
Nature Aging|April 28, 2023
Rare genetic coding variants associated with human longevity and protection against age-related diseasesJhih-Rong Lin, Patrick Sin-Chan, Valerio Napolioni, et al.
Nature Aging|August 28, 2024
Author Correction: Rare genetic coding variants associated with human longevity and protection against age-related diseasesJhih-Rong Lin, Patrick Sin-Chan, Valerio Napolioni, et al.
NPJ Genomic Medicine|July 18, 2023
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DSYingjie Zhao, Yujue Wang, Lijie Shi, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndromeJhih-Rong Lin, Daniella Miller, Dana Luong, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Nature Metabolism|July 29, 2020
Genetics of extreme human longevity to guide drug discovery for healthy ageingZhengdong D Zhang, Sofiya Milman, Jhih-Rong Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Polygenic prediction of human longevity on the supposition of pervasive pleiotropyM Reza Jabalameli, Jhih-Rong Lin, Quanwei Zhang, et al.
Scientific Reports|August 28, 2024
Polygenic prediction of human longevity on the supposition of pervasive pleiotropyM Reza Jabalameli, Jhih-Rong Lin, Quanwei Zhang, et al.
Cell Reports|November 10, 2021
Genomic expansion of Aldh1a1 protects beavers against high metabolic aldehydes from lipid oxidationQuanwei Zhang, Gregory Tombline, Julia Ablaeva, et al.
Developmental Neuroscience|October 13, 2024
Ultrarare Variants in DNA Damage Repair Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome or Acute Behavioral Regression in Neurodevelopmental DisordersJanet L Cunningham, Jennifer Frankovich, Robert A Dubin, et al.
Molecular Psychiatry|March 3, 2023
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophreniaJhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, et al.
Nature Aging|April 28, 2023
Rare genetic coding variants associated with human longevity and protection against age-related diseasesJhih-Rong Lin, Patrick Sin-Chan, Valerio Napolioni, et al.
Nature Aging|August 28, 2024
Author Correction: Rare genetic coding variants associated with human longevity and protection against age-related diseasesJhih-Rong Lin, Patrick Sin-Chan, Valerio Napolioni, et al.
NPJ Genomic Medicine|July 18, 2023
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DSYingjie Zhao, Yujue Wang, Lijie Shi, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndromeJhih-Rong Lin, Daniella Miller, Dana Luong, et al.
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